A STEREOSELECTIVE SYNTHESIS OF 3-SUBSTITUTED HEXAHYDROINDENO[2,1-B]PYRROLES VIA AN INTRAMOLECULAR AZOMETHINE YLIDE CYCLOADDITION

Authors
HARLING JD ORLEK BS
Citation
Jd. Harling et Bs. Orlek, A STEREOSELECTIVE SYNTHESIS OF 3-SUBSTITUTED HEXAHYDROINDENO[2,1-B]PYRROLES VIA AN INTRAMOLECULAR AZOMETHINE YLIDE CYCLOADDITION, Tetrahedron, 54(49), 1998, pp. 14905-14912
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
54
Issue
49
Year of publication
1998
Pages
14905 - 14912
Database
ISI
SICI code
0040-4020(1998)54:49<14905:ASSO3H>2.0.ZU;2-K
Abstract
3-Substituted hexahydroindeno[2,1-b]pyrroles were prepared in a stereo selective manner in high yield via an intramolecular azomethine ylide cycloaddition. Olefin geometry in the ylide precursor controlled the s tereochemistry at the 3-position. (C) 1998 Elsevier Science Ltd. All r ights reserved.